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Suppression tuning in noise-exposed rabbits.

Psychophysical, basilar-membrane (BM), and single nerve-fiber tuning curves, as well as suppression of distortion-product otoacoustic emissions (DPOAEs), all give rise to frequency tuning patterns with stereotypical features. Similarities and differences between the behaviors of these tuning functions, both in normal conditions and following various cochlear insults, have been documented. While neural tuning curves (NTCs) and BM tuning curves behave similarly both before and after cochlear insults known to disrupt frequency selectivity, DPOAE suppression tuning curves (STCs) do not necessarily mirror these responses following either administration of ototoxins [Martin et al., J. Acoust. Soc. Am. 104, 972-983 (1998)] or exposure to temporarily damaging noise [Howard et al., J. Acoust. Soc. Am. 111, 285-296 (2002)]. However, changes in STC parameters may be predictive of other changes in cochlear function such as cochlear immaturity in neonatal humans [Abdala, Hear. Res. 121, 125-138 (1998)]. To determine the effects of noise-induced permanent auditory dysfunction on STC parameters, rabbits were exposed to high-level noise that led to permanent reductions in DPOAE level, and comparisons between pre- and postexposure DPOAE levels and STCs were made. Statistical comparisons of pre- and postexposure STC values at CF revealed consistent basal shifts in the frequency region of greatest cochlear damage, whereas thresholds, Q10dB, and tip-to-tail gain values were not reliably altered. Additionally, a large percentage of high-frequency lobes associated with third tone interference phenomena, that were exhibited in some data sets, were dramatically reduced following noise exposure. Thus, previously described areas of DPOAE interference above f2 may also be studied using this type of experimental manipulation [Martin et al., Hear. Res. 136, 105-123 (1999); Mills, J. Acoust. Soc. Am. 107, 2586-2602 (2002)].

Acoustic Stimulation↗

An account of monaural phase sensitivity.

Listeners can detect phase differences between the envelopes of sounds occupying remote frequency regions, and between the fine structures of partials that interact within a single auditory filter. They are insensitive to phase differences between partials that differ sufficiently in frequency to preclude within-channel interactions. A new model is proposed that can account for all three of these findings, and which, unlike currently popular approaches, does not discard across-channel timing information. Sensitivity is predicted quantitatively by analyzing the output of a cochlear model using a spectro-temporal decomposition inspired by responses of neurons in the auditory cortex, and by computing a distance metric between the responses to two stimuli to be discriminated. Discriminations successfully modeled include phase differences between pairs of bandpass filtered harmonic complexes, and between pairs of sinusoidally amplitude modulated tones, discrimination between amplitude and frequency modulation, and discrimination of transient signals differing only in their phase spectra ("Huffman sequences").

Attention↗

Acoustic communication in two freshwater gobies: ambient noise and short-range propagation in shallow streams.

Noise is an important theoretical constraint on the evolution of signal form and sensory performance. In order to determine environmental constraints on the communication of two freshwater gobies Padogobius martensii and Gobius nigricans, numerous noise spectra were measured from quiet areas and ones adjacent to waterfalls and rapids in two shallow stony streams. Propagation of goby sounds and waterfall noise was also measured. A quiet window around 100 Hz is present in many noise spectra from noisy locations. The window lies between two noise sources, a low-frequency one attributed to turbulence, and a high-frequency one (200-500 Hz) attributed to bubble noise from water breaking the surface. Ambient noise from a waterfall (frequencies below 1 kHz) attenuates as much as 30 dB between 1 and 2 m, after which values are variable without further attenuation (i.e., buried in the noise floor). Similarly, courtship sounds of P. martensii attenuate as much as 30 dB between 5 and 50 cm. Since gobies are known to court in noisy as well as quiet locations in these streams, their acoustic communication system (sounds and auditory system) must be able to cope with short-range propagation dictated by shallow depths and ambient noise in noisy locations.

Acoustics↗

Informational masking: counteracting the effects of stimulus uncertainty by decreasing target-masker similarity.

Previous work has indicated that target-masker similarity, as well as stimulus uncertainty, influences the amount of informational masking that occurs in detection, discrimination, and recognition tasks. In each of five experiments reported in this paper, the detection threshold for a tonal target in random multitone maskers presented simultaneously with the target tone was measured for two conditions using the same set of five listeners. In one condition, the target was constructed to be "similar" (S) to the masker; in the other condition, it was constructed to be "dissimilar" (D) to the masker. The specific masker varied across experiments, but was constant for the two conditions. Target-masker similarity varied in dimensions such as duration, perceived location, direction of frequency glide, and spectro-temporal coherence. Group-mean results show large decreases in the amount of masking for the D condition relative to the S condition. In addition, individual differences (a hallmark of informational masking) are found to be much greater in the S condition than in the D condition. Furthermore, listener vulnerability to informational masking is found to be consistent to at least a moderate degree across experiments.

Acoustic Stimulation↗

The effects of a high-frequency suppressor on tuning curves and derived basilar-membrane response functions.

Forward-masked psychophysical tuning curves were obtained using a fixed, low-level signal at a frequency of 4 kHz, and masker frequencies of 2.0, 2.5, 3.0, 3.5, 3.75, 4.0, 4.25, 4.5, 4.75, 5.0, and 5.5 kHz, at masker-signal gaps of 20, 30, 40, 60, 80, and 100 ms. An adaptive two-interval, two alternative forced-choice (21-2AFC) procedure was used to obtain the masker level at threshold. This procedure was repeated with the addition of a 4.75-kHz suppressor at 50 or 60 dB SPL, gated with the masker. Tuning curves were broader, and estimates of compression and gain from derived input/output functions were decreased in the presence of a suppressor as compared to the no-suppressor condition. The results are consistent with physiological results, which show that suppression leads to a broadening of tuning curves and a partial linearization of the midlevel portion of the basilar-membrane input/output function.

Acoustic Stimulation↗

Examination of a linear model in an informational masking study.

When multitone maskers are used in a two-interval, forced choice experiment, the amount of masking is larger when the masker is randomly chosen on each presentation interval compared to on each trial (the same masker in the two listening intervals). These conditions are referred to as having within- versus between-trial randomization. If it is assumed that an observer's ultimate detection decision depends on a single decision variable (DV), it is probable that the DV's variance will be substantially larger in the within-trial randomization condition compared to the between-trial randomization condition. The goal of the current experiment is to evaluate the degree to which this stimulus-based change in DV variance can account for the difference in thresholds in the within-versus between-trial randomization conditions. Thresholds are measured for the detection of a tone added to a six-component masker in between- and within-trial randomization conditions. The slopes of the psychometric functions provide an estimate of the variance in the DV for the between- and within-trial randomization conditions. Additionally, a channel model is fitted to the psychophysical results in the within-trial randomization condition. The resulting model is then used to predict the value of the DV for each trial, and ultimately to estimate the proportion of the total variance in the within-trial randomization condition that is attributable to changes in maskers across intervals. The variance of the DV in the between-trial randomization condition accounted for approximately 65% of the total variance in the DV in the within-trial randomization condition. Stimulus-based interval-by-interval masker randomization accounted for approximately 20% of the total variance of the within-trial randomization DV. The remaining 15% of the DV variance in the within-trial randomization condition remained unaccounted for. This result is fairly stable whether the maskers are drawn from a small versus large pool of potential maskers.

Attention↗

Intensity discrimination and increment detection in cochlear-implant users.

Intensity difference limens (DLs) were measured in users of the Nucleus 22 and Clarion v1.2 cochlear implants and in normal-hearing listeners to better understand mechanisms of intensity discrimination in electric and acoustic hearing and to evaluate the possible role of neural adaptation. Intensity DLs were measured for three modes of presentation: gated (intensity increments gated synchronously with the pedestal), fringe (intensity increments delayed 250 or 650 ms relative to the onset of the pedestal), and continuous (intensity increments occur in the presence of a pedestal that is played throughout the experimental run). Stimuli for cochlear-implant listeners were trains of biphasic pulses; stimuli for normal-hearing listeners were a 1-kHz tone and a wideband noise. Clarion cochlear-implant listeners showed level-dependent effects of presentation mode. At low pedestal levels, gated thresholds were generally similar to thresholds obtained in the fringe and continuous conditions. At higher pedestal levels, however, the fringe and continuous conditions produced smaller intensity DLs than the gated condition, similar to the gated-continuous difference in intensity DLs observed in acoustic hearing. Nucleus cochlear-implant listeners did not show consistent threshold differences for the gated and fringe conditions, and were not tested in the continuous condition. It is not clear why a difference between gated and fringe thresholds occurred for the Clarion but not the Nucleus subjects. Normal-hearing listeners showed improved thresholds for the continuous condition relative to the gated condition, but the effect was larger for the 1-kHz tonal carrier than for the noise carrier. Findings suggest that adaptation occurring central to the inner hair cell synapse mediates the gated-continuous difference observed in Clarion cochlear-implant listeners and may also contribute to the gated-continuous difference in acoustic hearing.

Acoustic Stimulation↗

Transient elastography in anisotropic medium: application to the measurement of slow and fast shear wave speeds in muscles.

From the measurement of a low frequency (50-150 Hz) shear wave speed, transient elastography evaluates the Young's modulus in isotropic soft tissues. In this paper, it is shown that a rod source can generate a low frequency polarized shear strain waves. Consequently this technique allows to study anisotropic medium such as muscle. The evidence of the polarization of low frequency shear strain waves is supported by both numeric simulations and experiments. The numeric simulations are based on theoretical Green's functions in isotropic and anisotropic media (hexagonal system). The experiments in vitro led on beef muscle proves the pertinent of this simple anisotropic pattern. Results in vivo on man biceps shows the existence of slow and fast shear waves as predicted by theory.

Acoustic Stimulation↗

Effects of simulated cochlear-implant processing on speech reception in fluctuating maskers.

This study investigated the effects of simulated cochlear-implant processing on speech reception in a variety of complex masking situations. Speech recognition was measured as a function of target-to-masker ratio, processing condition (4, 8, 24 channels, and unprocessed) and masker type (speech-shaped noise, amplitude-modulated speech-shaped noise, single male talker, and single female talker). The results showed that simulated implant processing was more detrimental to speech reception in fluctuating interference than in steady-state noise. Performance in the 24-channel processing condition was substantially poorer than in the unprocessed condition, despite the comparable representation of the spectral envelope. The detrimental effects of simulated implant processing in fluctuating maskers, even with large numbers of channels, may be due to the reduction in the pitch cues used in sound source segregation, which are normally carried by the peripherally resolved low-frequency harmonics and the temporal fine structure. The results suggest that using steady-state noise to test speech intelligibility may underestimate the difficulties experienced by cochlear-implant users in fluctuating acoustic backgrounds.

Acoustic Stimulation↗

The relationship between acoustic structure and semantic information in Diana monkey alarm vocalization.

Mammalian vocal production mechanisms are still poorly understood despite their significance for theories of human speech evolution. Particularly, it is still unclear to what degree mammals are capable of actively controlling vocal-tract filtering, a defining feature of human speech production. To address this issue, a detailed acoustic analysis on the alarm vocalization of free-ranging Diana monkeys was conducted. These vocalizations are especially interesting because they convey semantic information about two of the monkeys' natural predators, the leopard and the crowned eagle. Here, vocal tract and sound source parameter in Diana monkey alarm vocalizations are described. It is found that a vocalization-initial formant downward transition distinguishes most reliably between eagle and leopard alarm vocalization. This finding is discussed as an indication of articulation and alternatively as the result of a strong nasalization effect. It is suggested that the formant modulation is the result of active vocal filtering used by the monkeys to encode semantic information, an ability previously thought to be restricted to human speech.

Acoustics↗

Basilar-membrane responses to multicomponent (Schroeder-phase) signals: understanding intensity effects.

Harmonic complexes comprised of the same spectral components in either positive-Schroeder (+Schr) or negative-Schroeder (-Schr) phase [see Schroeder, IEEE Trans. Inf. Theory 16, 85-89 (1970)] have identical long-term spectra and similar waveform envelopes. However, localized patterns of basilar-membrane (BM) excitation can be quite different in response to these two stimuli. Measurements in chinchillas showed more modulated (peakier) BM excitation for +Schr than -Schr complexes [Recio and Rhode, J. Acoust. Soc. Am. 108, 2281-2298 (2000)]. In the current study, laser velocimetry was used to examine BM responses at a location tuned to approximately 17 kHz in the basal turn of the guinea-pig cochlea, for +Schr and -Schr complexes with a 203-Hz fundamental frequency and including 101 equal-amplitude components from 2031 to 22,344 Hz. At 35-dB SPL, +Schr response waveforms showed greater amplitude modulation than -Schr responses. With increasing stimulation level, internal modulation decreased for both complexes. To understand the observed phenomena quantitatively, responses were predicted on the basis of a linearized model of the cochlea. Prediction was based on an "indirect impulse response" measured in the same animal. Response waveforms for Schroeder-phase signals were accurately predicted, provided that the level of the indirect impulse used in prediction closely matched the level of the Schroeder-phase stimulus. This result confirms that the underlying model, which originally was developed for noise stimuli, is valid for stimuli that produce completely different response waveforms. Moreover, it justifies explanation of cochlear filtering (i.e., differential treatment of different frequencies) in terms of a linear system.

Animals↗

Vertical-plane sound localization probed with ripple-spectrum noise.

Ripple-spectrum stimuli were used to investigate the scale of spectral detail used by listeners in interpreting spectral cues for vertical-plane localization. In three experiments, free-field localization judgments were obtained for 250-ms, 0.6-16-kHz noise bursts with log-ripple spectra that varied in ripple density, peak-to-trough depth, and phase. When ripple density was varied and depth was held constant at 40 dB, listeners' localization error rates increased most (relative to rates for flat-spectrum targets) for densities of 0.5-2 ripples/oct. When depth was varied and density was held constant at 1 ripple/oct, localization accuracy was degraded only for ripple depths > or = 20 dB. When phase was varied and density was held constant at 1 ripple/oct and depth at 40 dB, three of five listeners made errors at consistent locations unrelated to the ripple phase, whereas two listeners made errors at locations systematically modulated by ripple phase. Although the reported upper limit for ripple discrimination is 10 ripples/oct [Supin et al., J. Acoust. Soc. Am. 106, 2800-2804 (1999)], present results indicate that details finer than 2 ripples/oct or coarser than 0.5 ripples/oct do not strongly influence processing of spectral cues for sound localization. The low spectral-frequency limit suggests that broad-scale spectral variation is discounted, even though components at this scale are among those contributing the most to the shapes of directional transfer functions.

Acoustic Stimulation↗

Effectiveness of narrow-band versus tonal off-frequency maskers.

The present study was a follow-up to a pilot study in which it was found that a 500-Hz-wide narrow-band noise (NBN) masker produced more masking than a tonal (T) masker for signal frequencies both above and below the masker frequency. The aim of the present study was to determine to what extent these results were influenced by an interaction of the relatively rapid temporal envelope fluctuations of the NBN and the short (10-ms) duration of the signal. In the first experiment, the masking produced by a regular NBN, a low-noise noise (LNN), and a T was compared. The LNN produced less masking than the NBN, and about as much as the T, suggesting that the inherent amplitude fluctuations in the NBN were largely responsible for the greater masking produced by that masker. In the second experiment, the masking produced by a regular NBN was compared with that by a T for a signal duration of 10 or 200 ms. The difference in masking between the two maskers was reduced or eliminated when the signal duration was 200 ms, because the threshold in the presence of the NBN masker decreased more with increasing signal duration. This could reflect a decreased "confusion" between the signal and the inherent fluctuations of the NBN masker.

Acoustic Stimulation↗

The effects of the amplitude distribution of equal energy exposures on noise-induced hearing loss: the kurtosis metric.

Seventeen groups of chinchillas with 11 to 16 animals/group (sigmaN = 207) were exposed for 5 days to either a Gaussian (G) noise or 1 of 16 different non-Gaussian (non-G) noises at 100 dB(A) SPL. All exposures had the same total energy and approximately the same flat spectrum but their statistical properties were varied to yield a series of exposure conditions that varied across a continuum from G through various non-G conditions to pure impact noise exposures. The non-G character of the noise was produced by inserting high level transients (impacts or noise bursts) into the otherwise G noise. The peak SPL of the transients, their bandwidth, and the intertransient intervals were varied, as was the rms level of the G noise. The statistical metric, kurtosis (beta), computed on the unfiltered noise beta(t), was varied 3 < or = beta(t) < or = 105. Brainstem auditory evoked responses were used to estimate hearing thresholds and surface preparation histology was used to determine sensory cell loss. Trauma, as measured by asymptotic and permanent threshold shifts (ATS, PTS) and by sensory cell loss, was greater for all of the non-G exposure conditions. Permanent effects of the exposures increased as beta(t) increased and reached an asymptote at beta(t) approximately 40. For beta(t) > 40 varying the interval or peak histograms did not alter the level of trauma, suggesting that, in the chinchilla model, for beta(t) > 40 an energy metric may be effective in evaluating the potential of non-G noise environments to produce hearing loss. Reducing the probability of a transient occurring could reduce the permanent effects of the non-G exposures. These results lend support to those standards documents that use an energy metric for gauging the hazard of exposure but only after applying a "correction factor" when high level transients are present. Computing beta on the filtered noise signal [beta(f)] provides a frequency specific metric for the non-G noises that is correlated with the additional frequency specific outer hair cell loss produced by the non-G noise. The data from the abundant and varied exposure conditions show that the kurtosis of the amplitude distribution of a noise environment is an important variable in determining the hazards to hearing posed by non-Gaussian noise environments.

Acoustic Stimulation↗

Asymmetry of masking between complex tones and noise: partial loudness.

This experiment examined the partial masking of periodic complex tones by a background of noise, and vice versa. The tones had a fundamental frequency (F0) of 62.5 or 250 Hz, and components were added in either cosine phase (CPH) or random phase (RPH). The tones and the noise were bandpass filtered into the same frequency region, from the tenth harmonic up to 5 kHz. The target alone was alternated with the target and the background; for the mixture, the background and target were either gated together, or the background was turned on 400 ms before, and off 200 ms after, the target. Subjects had to adjust the level of either the target alone or the target in the background so as to match the loudness of the target in the two intervals. The overall level of the background was 50 dB SPL, and loudness matches were obtained for several fixed levels of the target alone or in the background. The resulting loudness-matching functions showed clear asymmetry of partial masking. For a given target-to-background ratio, the partial loudness of a complex tone in a noise background was lower than the partial loudness of a noise in a complex tone background. Expressed as the target-to-background ratio required to achieve a given loudness, the asymmetry typically amounted to 12-16 dB. When the F0 of the complex tone was 62.5 Hz, the asymmetry of partial masking was greater for CPH than for RPH. When the F0 was 250 Hz, the asymmetry was greater for RPH than for CPH. Masked thresholds showed the same pattern as for partial masking for both F0's. Onset asynchrony had some effect on the loudness matching data when the target was just above its masked threshold, but did not significantly affect the level at which the target in the background reached its unmasked loudness. The results are interpreted in terms of the temporal structure of the stimuli.

Adult↗

Representation of the voice onset time (VOT) speech parameter in population responses within primary auditory cortex of the awake monkey.

Voice onset time (VOT) signifies the interval between consonant onset and the start of rhythmic vocal-cord vibrations. Differential perception of consonants such as /d/ and /t/ is categorical in American English, with the boundary generally lying at a VOT of 20-40 ms. This study tests whether previously identified response patterns that differentially reflect VOT are maintained in large-scale population activity within primary auditory cortex (A1) of the awake monkey. Multiunit activity and current source density patterns evoked by the syllables /da/ and /ta/ with variable VOTs are examined. Neural representation is determined by the tonotopic organization. Differential response patterns are restricted to lower best-frequency regions. Response peaks time-locked to both consonant and voicing onsets are observed for syllables with a 40- and 60-ms VOT, whereas syllables with a 0- and 20-ms VOT evoke a single response time-locked only to consonant onset. Duration of aspiration noise is represented in higher best-frequency regions. Representation of VOT and aspiration noise in discrete tonotopic areas of A1 suggest that integration of these phonetic cues occurs in secondary areas of auditory cortex. Findings are consistent with the evolving concept that complex stimuli are encoded by synchronized activity in large-scale neuronal ensembles.

Animals↗

Dichotic speech recognition in noise using reduced spectral cues.

It is generally accepted that the fusion of two speech signals presented dichotically is affected by the relative onset time. This study investigated the hypothesis that spectral resolution might be an additional factor influencing spectral fusion when the spectral information is split and presented dichotically to the two ears. To produce speech with varying degrees of spectral resolution, speech materials embedded in +5 dB S/N speech-shaped noise were processed through 6-12 channels and synthesized as a sum of sine waves. Two different methods of splitting the spectral information were investigated. In the first method, the odd-index channels were presented to one ear and the even-index channels to the other ear. In the second method the lower frequency channels were presented to one ear and the high-frequency channels to the other ear. Results indicated that spectral resolution did affect spectral fusion, and the effect differed across speech materials, with the sentences being affected the most. Sentences, processed through six or eight channels and presented dichotically in the low-high frequency condition were not fused as accurately as when presented monaurally. Sentences presented dichotically in the odd-even frequency condition were identified more accurately than when presented in the low-high condition.

Acoustic Stimulation↗